Canonical Allele Identifier: CA2483126515

Gene: IL10

Linked Data

• dbSNP Id: rs1674802568

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770726_206770732del , CM000663.2:g.206770726_206770732del	GRCh38
NC_000001.10:g.206944071_206944077del , CM000663.1:g.206944071_206944077del	GRCh37
NC_000001.9:g.205010694_205010700del	NCBI36
NG_012088.1:g.6765_6771del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+177_283+183del
ENST00000471071.2:c.123+177_123+183del	ENSP00000493073.2:n.123+177_123+183del
ENST00000659065.2:c.261+177_261+183del	ENSP00000499588.1:n.261+177_261+183del
ENST00000659642.2:c.261+177_261+183del	ENSP00000499509.1:n.261+177_261+183del
ENST00000664374.2:c.261+177_261+183del	ENSP00000499664.1:n.261+177_261+183del
ENST00000659065.1:c.261+177_261+183del	ENSP00000499588.1:n.261+177_261+183del
ENST00000659642.1:c.261+177_261+183del	ENSP00000499509.1:n.261+177_261+183del
ENST00000664374.1:c.261+177_261+183del	ENSP00000499664.1:n.261+177_261+183del
ENST00000367099.3:n.283+177_283+183del
ENST00000423557.1:c.378+177_378+183del MANE Select	ENSP00000412237.1:n.378+177_378+183del
ENST00000471071.1:n.293+177_293+183del
NM_000572.2:c.378+177_378+183del	NP_000563.1:n.378+177_378+183del
XM_011509506.1:c.378+177_378+183del	XP_011507808.1:n.378+177_378+183del
NM_000572.3:c.378+177_378+183del MANE Select	NP_000563.1:n.378+177_378+183del
NM_001382624.1:c.123+177_123+183del	NP_001369553.1:n.123+177_123+183del
NR_168466.1:n.437+177_437+183del